A citation-based method for searching scientific literature


List of co-cited articles
167 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


The emergence of an ethical duty to disclose genetic research results: international perspectives.
Bartha Maria Knoppers, Yann Joly, Jacques Simard, Francine Durocher. Eur J Hum Genet 2006
195
64

Disclosing individual genetic results to research participants.
Vardit Ravitsky, Benjamin S Wilfond. Am J Bioeth 2006
220
64



Implications of disclosing individual results of clinical research.
Ellen Wright Clayton, Lainie Friedman Ross. JAMA 2006
72
51

Reporting genetic results in research studies: summary and recommendations of an NHLBI working group.
Ebony B Bookman, Aleisha A Langehorne, John H Eckfeldt, Kathleen C Glass, Gail P Jarvik, Michael Klag, Greg Koski, Arno Motulsky, Benjamin Wilfond, Teri A Manolio,[...]. Am J Med Genet A 2006
160
51

Duty to disclose what? Querying the putative obligation to return research results to participants.
F A Miller, R Christensen, M Giacomini, J S Robert. J Med Ethics 2008
90
45

Managing incidental findings in human subjects research: analysis and recommendations.
Susan M Wolf, Frances P Lawrenz, Charles A Nelson, Jeffrey P Kahn, Mildred K Cho, Ellen Wright Clayton, Joel G Fletcher, Michael K Georgieff, Dale Hammerschmidt, Kathy Hudson,[...]. J Law Med Ethics 2008
463
45

Obligations in offering to disclose genetic research results.
Conrad V Fernandez, Charles Weijer. Am J Bioeth 2006
28
39

Returning genetic research results to individuals: points-to-consider.
Gaile Renegar, Christopher J Webster, Steffen Stuerzebecher, Lea Harty, Susan E Ide, Beth Balkite, Taryn A Rogalski-Salter, Nadine Cohen, Brian B Spear, Diane M Barnes,[...]. Bioethics 2006
69
35



Receiving a summary of the results of a trial: qualitative study of participants' views.
Mary Dixon-Woods, Clare Jackson, Kate C Windridge, Sara Kenyon. BMJ 2006
75
32

Best laid plans for offering results go awry.
Lisa S Parker. Am J Bioeth 2006
23
43



Public expectations for return of results from large-cohort genetic research.
Juli Murphy, Joan Scott, David Kaufman, Gail Geller, Lisa LeRoy, Kathy Hudson. Am J Bioeth 2008
201
29

Ethical and practical guidelines for reporting genetic research results to study participants: updated guidelines from a National Heart, Lung, and Blood Institute working group.
Richard R Fabsitz, Amy McGuire, Richard R Sharp, Mona Puggal, Laura M Beskow, Leslie G Biesecker, Ebony Bookman, Wylie Burke, Esteban Gonzalez Burchard, George Church,[...]. Circ Cardiovasc Genet 2010
281
29

Informing study participants of research results: an ethical imperative.
Conrad V Fernandez, Eric Kodish, Charles Weijer. IRB 2003
133
25

Informed consent for population-based research involving genetics.
L M Beskow, W Burke, J F Merz, P A Barr, S Terry, V B Penchaszadeh, L O Gostin, M Gwinn, M J Khoury. JAMA 2001
184
25


Disclosure of individual genetic data to research participants: the debate reconsidered.
Annelien L Bredenoord, Hester Y Kroes, Edwin Cuppen, Michael Parker, Johannes J M van Delden. Trends Genet 2011
149
25




Informing clinical trial participants about study results.
Ann H Partridge, Eric P Winer. JAMA 2002
120
22



Considerations and costs of disclosing study findings to research participants.
Conrad V Fernandez, Chris Skedgel, Charles Weijer. CMAJ 2004
63
19

Research ethics and the challenge of whole-genome sequencing.
Amy L McGuire, Timothy Caulfield, Mildred K Cho. Nat Rev Genet 2008
141
19

Subjects matter: a survey of public opinions about a large genetic cohort study.
David Kaufman, Juli Murphy, Joan Scott, Kathy Hudson. Genet Med 2008
157
19


Offering individual genetic research results: context matters.
Laura M Beskow, Wylie Burke. Sci Transl Med 2010
129
19

Managing incidental findings and research results in genomic research involving biobanks and archived data sets.
Susan M Wolf, Brittney N Crock, Brian Van Ness, Frances Lawrenz, Jeffrey P Kahn, Laura M Beskow, Mildred K Cho, Michael F Christman, Robert C Green, Ralph Hall,[...]. Genet Med 2012
296
19

Incidental findings in human subjects research: what do investigators owe research participants?
Franklin G Miller, Michelle M Mello, Steven Joffe. J Law Med Ethics 2008
71
19

ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing.
Robert C Green, Jonathan S Berg, Wayne W Grody, Sarah S Kalia, Bruce R Korf, Christa L Martin, Amy L McGuire, Robert L Nussbaum, Julianne M O'Daniel, Kelly E Ormond,[...]. Genet Med 2013
19

When do genetic researchers have a duty to recontact study participants?
Christopher H Wade, Andrea L Kalfoglou. Am J Bioeth 2006
14
35

Relationships with test-tubes: where's the reciprocity?
Kelly Fryer-Edwards, Stephanie M Fullerton. Am J Bioeth 2006
15
33

Do patients participating in clinical trials want to know study results?
Ann H Partridge, Harold J Burstein, Rebecca S Gelman, P Kelly Marcom, Eric P Winer. J Natl Cancer Inst 2003
64
16

Issues of consent and feedback in a genetic epidemiological study of women with breast cancer.
M P M Richards, M Ponder, P Pharoah, S Everest, J Mackay. J Med Ethics 2003
43
16


Impact on survivors of retinoblastoma when informed of study results on risk of second cancers.
Charlene J Schulz, Mary P Riddle, Heiddis B Valdimirsdottir, David H Abramson, Charles A Sklar. Med Pediatr Oncol 2003
51
16

Disclosure of genetic information obtained through research.
Kimberly A Quaid, Nenette M Jessup, Eric M Meslin. Genet Test 2004
24
20




The incidentalome: a threat to genomic medicine.
Isaac S Kohane, Daniel R Masys, Russ B Altman. JAMA 2006
213
16


What is a meaningful result? Disclosing the results of genomic research in autism to research participants.
Fiona Alice Miller, Robin Zoe Hayeems, Jessica Peace Bytautas. Eur J Hum Genet 2010
44
16



Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.